All individuals with variants in gene FOLR1

6 entries on 1 page. Showing entries 1 - 6.
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00081087 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - NCFTD Neurodegeneration due to cerebral folate transport deficiency (OMIM:613068) 1 1 Daniel Trujillano
00180176 29286531-Pat28 PubMed: Tumienė 2018 - - - (Slovenia) - - - - - ? Epileptic encephalopathy (HP:0200134), global developmental delay (HP:0001263). 1 1 Johan den Dunnen
00290530 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 49 Mohammed Faruq
00374738 S-1933 PubMed: Ganapathy 2019 - - - India - - - - - ? - 1 1 Johan den Dunnen
00468028 FamPat1A PubMed: Ohba 2013 2-generation family, affected brother/sister, unaffected heterozygous carrier parents M - Japan - - - - - ? see paper; ..., ataxia; no dysmetria; no oculomotor apraxia; intention tremor; developmental delay; intellectual disability; slurred speech, three-word sentences; mild hypotonia/spastic lower limbs; pyramidal sign; no extrapyramidal sign; no peripheral neuropathy; epileptic seizure; low IgG; MRI cerebellar atrophy/hypoplasia, mild brainstem atrophy, cerebral white matter atrophy, calcification at subcortical white matter 2 2 Johan den Dunnen
00468029 FamPat1B PubMed: Ohba 2013 sister F - Japan - - - - - ? see paper; ..., ataxia; no dysmetria; no oculomotor apraxia; intention tremor; developmental delay; intellectual disability; slurred speech, three-word sentences; mild hypotonia; no pyramidal sign; no extrapyramidal sign; epileptic seizure;  ; MRI cerebellar atrophy/hypoplasia, no brainstem atrophy, calcification at basal ganglia and subcortical white matter 2 1 Johan den Dunnen
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